• QA Technical Writing Management NS &E

    ABBTECH Professional Resources, Inc. (Oak Ridge, TN)
    **Job Summary:** The primary role of the UPF Startup Technical Writer will be to support the Startup team with Test Packages. To ensure technical editing, graphics, ... editorial changes. Provide accurate input to the Startups Lead Technical Writer to prevent delays in testing activities. **Major Responsibilities:** Take detailed… more
    ABBTECH Professional Resources, Inc. (05/15/25)
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  • Future Opportunities- Join Our Talent Pipeline…

    AbbVie (Mettawa, IL)
    …talent pipeline and considered for future opportunities. About the role: The Principal Medical Writer is responsible for providing writing support and advanced ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...required or in a related area such as quality, regulatory , publications, clinical research, or product support/R&D. + 2… more
    AbbVie (07/14/25)
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  • Workday Administrator | Remote

    Clay Lacy Aviation (Van Nuys, CA)
    …$88,000 - $140,000 per year. This position includes comprehensive medical , dental, and vision benefits. Duties and Responsibilities System Implementation ... KPIs, and analytical reports with business and analytics leaders, using report writer and calculated fields to support strategy, planning and compliance. + Provide… more
    Clay Lacy Aviation (06/21/25)
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  • Submission Ready Standards Specialist

    Takeda Pharmaceuticals (Boston, MA)
    …providing Submission Ready Standard Application during the preparation of high quality regulatory submissions and a wide range of supporting documentation across the ... the submission build activities for both paper and electronic regulatory submissions, ensuring submissions are built with submission-ready documents, creating… more
    Takeda Pharmaceuticals (08/09/25)
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  • Utilization and Appeals Manager

    Catholic Health Services (Melville, NY)
    …opportunities for improvement from both internal and external sources including regulatory agencies. Responsibilities include but not limited to: Receives, manages ... provides clinical reviews and/or submissions as required by contractual or regulatory requirements. Researches initial denial, identifying reason for the denial and… more
    Catholic Health Services (07/24/25)
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  • Internal Audit Quality Manager, Professional…

    Amazon (Arlington, VA)
    …Key job responsibilities Key responsibilities include leading board, executive, and regulatory reporting; metrics development and monitoring for the Internal Audit ... and board or external reporting submissions and other audit activities. Strong technical writer /editor with attention to details. A day in the life Demonstrate high… more
    Amazon (07/30/25)
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  • Environmental Engineer

    Access Dubuque (Dubuque, IA)
    …Work with customers to ensure systems meet business needs. + Develop regulatory submittals and internal reports. Oversee the preparation of submittals by ... consultants/service providers. Interface with regulatory personnel during audits and to clarify program needs...Fixed Contributions & Company Matching * Profit Sharing * Medical , dental, prescription, vision coverage * Tax-advantaged accounts for… more
    Access Dubuque (08/01/25)
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  • Sr Contract Coordinator

    Exelon (Plymouth Meeting, PA)
    …& guidelines in order to satisfy corporate, business unit, municipal and regulatory requirements. Maintains an environment that promotes safety, diversity, and high ... guidelines in order to satisfy corporate, business unit, municipal and regulatory requirements. Maintains an environment that promotes safety, diversity and… more
    Exelon (08/02/25)
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  • Lead, Technology Risk

    Coinbase (St. Paul, MN)
    …GRC teams, Legal and Compliance for risks, assessments, and reporting to meet regulatory requirements. * Support audit and regulatory inspections: Support data ... and qualitative data analytics tooling. * Clear/concise communicator and writer ; experience drafting/operationalizing project plans across stakeholders, holding teams… more
    Coinbase (08/09/25)
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  • Senior Process Engineer I, Ctto Drug Product

    Bristol Myers Squibb (Summit, NJ)
    …for significant documents such as validation activities, author content for regulatory submissions. + Ensure technical and manufacturing requirements are addressed ... large data sets in support of batch history sections for regulatory submissions. Proficiency in data management/statistical analysis software, including Excel, JMP,… more
    Bristol Myers Squibb (08/09/25)
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